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      Novel nonsense and splice site mutations in CRB1 gene in two Japanese patients with early-onset retinal dystrophy.

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          Abstract

          To report novel mutations in the CRB1 gene in two patients with early-onset retinal dystrophy (EORD) and the longitudinal clinical course of EORD.

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          Author and article information

          Journal
          Doc Ophthalmol
          Documenta ophthalmologica. Advances in ophthalmology
          Springer Science and Business Media LLC
          1573-2622
          0012-4486
          Feb 2015
          : 130
          : 1
          Affiliations
          [1 ] Department of Ophthalmology, Kinki University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama City, Osaka, 589-8511, Japan, kuniyoshi-kazuki@umin.net.
          Article
          10.1007/s10633-014-9464-8
          25323024
          4a3c4b1b-32b3-49e4-834a-8ca8e6d1007c
          History

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